In order to study the effect of inoculation with mycorrhiza and fertilization with plant residues on the growth of plants, we used two factors: the first two levels of mycorrhiza inoculation, Glumus mossea (0 and 10 g.pot-1) and the second factor, four levels of plant residues (10 g.pot-1) celery plant residues, 10 g pot-1 mint residues, and 10 g pot-1 black bean seed residues. Mychorrizal treatment (10 g pot-1) increased the number of mycorrhiza spores and the infection percentage of mycorrhizal by 917.44% and 13088.23%, respectively; celery treatment (10 g.pot-1) increased the chlorophyll index in the leaves and height of the chard plant by 31.34% and 94.04%, respectively; and black seed treatment (10 g.pot-1) increased the percentage of dry matter in the leaves and the percentage of carbohydrates in the leaves by 81.51% and 53.36%, respectively.The results showed the bilateral interactions between the experimental factors that the treatment of mycorrhizal inoculation exceeded (10 g pot-1) and celery (10 g.pot-1) residues in most of the study parameters in each of the Total Chlorophyll index in the leaves (SPAD), plant height, percentage of dry matter in the leaves (%), percentage of carbohydrates in the leaves, number of mycorrhiza spores, and infection percentage of mycorrhizal were (46%, 150.89%, 139.88%, 92.07%, 3283.45%, and 4000%, respectively, compared to the control treatment.
Two simple methods for the determination of eugenol were developed. The first depends on the oxidative coupling of eugenol with p-amino-N,N-dimethylaniline (PADA) in the presence of K3[Fe(CN)6]. A linear regression calibration plot for eugenol was constructed at 600 nm, within a concentration range of 0.25-2.50 μg.mL–1 and a correlation coefficient (r) value of 0.9988. The limits of detection (LOD) and quantitation (LOQ) were 0.086 and 0.284 μg.mL–1, respectively. The second method is based on the dispersive liquid-liquid microextraction of the derivatized oxidative coupling product of eugenol with PADA. Under the optimized extraction procedure, the extracted colored product was determined spectrophotometrically at 618 nm. A l
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